Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NOBLES-LAI IMAGING SYSTEM

K-Number: K920026 · 1992-07-28

Decision Date1992-07-28
Product CodeFET
Advisory CommitteeGU
DecisionUnknown

Device Summary

NOBLES-LAI IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nobles-Lai Engineering, Inc.. It received FDA 510(k) clearance on 1992-07-28 under 510(k) number K920026. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the NOBLES-LAI IMAGING SYSTEM?

NOBLES-LAI IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1992-07-28. The listed applicant is Nobles-Lai Engineering, Inc.. The 510(k) number is K920026.

When did NOBLES-LAI IMAGING SYSTEM receive FDA 510(k) clearance?

NOBLES-LAI IMAGING SYSTEM received FDA 510(k) clearance on 1992-07-28, under 510(k) number K920026.

Who is the listed applicant for NOBLES-LAI IMAGING SYSTEM?

The FDA 510(k) record lists Nobles-Lai Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOBLES-LAI IMAGING SYSTEM?

The FDA product code for NOBLES-LAI IMAGING SYSTEM is FET.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Nobles-Lai Engineering, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FET)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑